Tian Hongqi's personality career.

Education experience:1Graduated from Chemistry Department of Sichuan University in July 1990,1Ph.D. from Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences in June 1998.

Business experience

From 20 10 to present, professor and doctoral supervisor of School of Pharmacy, Nankai University;

Since June 2006, 5438, Ali Pharmaceutical Company, senior research scientist;

1September 1998 to May 2006, 5438+0, postdoctoral fellow, Department of Chemistry, University of Colorado, USA;

1July 1990 to1August 1993 Assistant Engineer, Institute of Photosensitive Chemistry, former Ministry of Chemical Industry.

My specialty

Through the study of structure-activity relationship, the lead compounds were optimized and new drugs were developed. Have a certain understanding of the target receptor in the field of receptor protein kinase, and accordingly put forward the project of developing new drugs for cancer treatment; Has the specialty of developing new organic reaction methodology research; Has the specialty of studying the industrial process of organic compounds; Familiar with various analytical instruments (such as NMR, LC-MS, LC, GC, IR and MS). ) to determine the structure and other required characterization of organic compounds.

Published articles

1. Optimize the structure-activity relationship of SERMs for uterine antagonism and ovarian safety. T. Richardson; S. frank; M. Wang; C. Clark; S Jones; B. should; D. Coleman; O Wallace; T. Shepard; R. Daley; A. Palko Witz; A. Gaither; H. Bryant; Heng Ke; I. Cohen; D. Roudman; D. McCann; D. Coutants. oldham; Hummel; Fang Gang; R. Hinkling; G. Lewis; H. Tian; J. dodge Bioorganic and bioengineering. Medicinal Chemistry Letters, 2007, 17( 13), 3544-3549.

2. A selective estrogen receptor modulator designed to treat uterine leiomyoma with unique tissue specificity for rat uterus and ovary. Hummel; A. Gaither; H. Bryant; I. Cohen; R. Daley; Fang Gang; S. frank; R. Hinkling; S Jones; G. Lewis; D. McCann; D. Roudman; T. Shepard; H. Tian; O Wallace; M. Wang; Y. Wang; J. dodge Journal of Medicinal Chemistry, 2005, 48(22), 6772-6775.

3. Asymmetric Strake reaction of G-keto acid. It is easy to enter α-substituted and α, g- disubstituted glutamic acid. Tang, Tian, Ma *, Tetrahedron, 2004,60 (46), 10547- 10552.

4. Asymmetric synthesis of (S)-1-aminoindane-1,5- dicarboxylic acid and related analogues. Ma, Ke, Tian, Wang, Cheng, Tetrahedron: Asymmetric, 2002, 13(9), 96 1-969.

5. Design a new chiral ketone catalyst. Enantioselective epoxidation of cis-and terminal olefins, Tian, She, Shu, Shu, Shi. Chemistry. , 2002, 67(8), 2435-2446.

6. Enantioselective epoxidation of terminal olefins by chiral dioxane. Ritter. , 200 1, 3( 12), 1929- 193 1.

7. Electron probe of asymmetric epoxidized ketone catalyst. Looking for a more powerful catalyst. Ritter. , 200 1, 3(5), 7 15-7 18.

8. enantioselective epoxidation of cis-olefins by chiral dioxane, Tian, She, Shu, Shu, Shi. Chemistry. Socialist, 2000,122,11551-1552.

9. Benzylidene compounds are oxidized to ketone, horse, summer, field and tetrahedron by m-chloroperoxybenzoic acid and oxygen. 1999, 40(50), 89 15-89 17.

10. enantioselective synthesis of a-substituted glutamic acid and a, g- disubstituted glutamic acid by asymmetric Strecker reaction, D. Ma *, G. Tang, H. Tian, G. Zou, Tetrahedron.1999,40 (31).

Asymmetric Strecker type reaction of 1 1.α- aryl ketone. Synthesis of metabotropic glutamate receptor antagonists s-aM4CPG, s-MPPG, s-AIDA and s-APICA. Chemistry. , 1999, 64( 1), 120- 125.

12. stereoselective synthesis of s-MPPG, s-MTPG and s-(+)-aM4CPG from R-4- hydroxyphenylglycine. Socialist Perkin. Transaction 1,1997,23,3493-3496.

13. Synthesis and biological activity of cyclic analogues of sum as metabotropic receptor antagonists. & Medicine. Chemistry. Ritter. , 1997, 7(9), 1 195- 1 198.

14. Asymmetric synthesis of metabotropic glutamate receptor selective antagonist (+)-4CPMG. Tetrahedron: asymmetric,1996,7 (6), 1567- 1570.

Published patent

1. Preparation of pyrrolidone and piperidone derivatives as 1 1-β- hydroxysteroid dehydrogenase 1 inhibitors. Mr. T. Aicher Cicarelli; C. gautier; R. Hinkling; H. Tian; O Wallace.

2. Preparation of pyrrolidone and piperidone as 1 1-β- hydroxysteroid dehydrogenase 1 inhibitors. Mr. T. Aicher Cicarelli; C. gautier; R. Hinkling; H. Tian; O Wallace; Krasucki; J. Allen.

3. Preparation of cycloalkyllactam derivatives as 1 1-β- hydroxysteroid dehydrogenase 1 inhibitors, especially n- substituted pyrrolidine -2- one. Mr. T. Aicher Cicarelli; C. gautier; R. Hinkling; H. Tian; O Wallace; Z. Chen; T. Marbury; J. McCowan; Snyder; L. Wennerowski; J. Allen.

4. Heterobicyclic thiophene compounds as tyrosine kinase inhibitors and their preparation and use. J. Blake; Boyd; J. demis; J. Gaudino; A. Marlowe; J. Seoa. Thomas; Tian. US 2007 197537.

5. Heterobicyclic pyrazole compounds as inhibitors of Met tyrosine kinase, and their preparation and use. J. Blake; Boyd; F. Cohen; J. demis; Fang Gang; J. Gaudino; T. Kaplan; A. Marlowe; J. Seoa. Thomas; H. Tian; W. yang

6. Cyclohexylpyrazole-lactam derivatives as β -hydroxysteroid dehydrogenase 1 inhibitors. T. Aicherp. anzevino; Krasucki; R. Li; T. Marbury; A. Said; Snyder; G. Stephenson; H. Tian; O Wallace; L. Wennerowski; Xu yuanchong. (Note: In addition to the countries specified in WO, the patent has been applied for in another 16 countries).

7. Preparation of quinoline derivatives as tyrosine kinase inhibitors. J. Gaudino; Boyd; A. Marlowe; T. Kaplan; Fang Gang; J.seoh. Tian; J. Blake; K. Koch

8. Heterobicyclic pyrazolopyridine compounds as tyrosine kinase inhibitors and their preparation and use. J. Blake; Boyd; F. Cohen; J. demis; Fang Gang; J. Gaudino; A. Marlowe; J. Seoa. Thomas; H. Tian; W. yang Has been applied.

9. Heterobicyclic azaindole compounds as tyrosine kinase inhibitors and their preparation and use. J. Blake; Boyd; Fang Gang; J. Gaudino; Tian. The manuscript is being prepared.